HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 18762668, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 3-Amino-2,6-piperidinedione | HCID 134508 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 18762668 | HCID 18762668 | — |
Reaction Steps
A solution of 0.50 g 3-aminopiperidine-2,6-dione (K. Fickentscher, Arch. Pharm. 1974, 307, 840-844), 1.5 ml triethylamine and 0.4 ml benzyl bromide was stirred for 20 h at 20° C. It was then evaporated, the residue taken up in 50 ml aqueous potassium carbonate solution (10% K2CO3) and the solution extracted twice with 40 ml ethyl acetate each. The organic phases were washed with 50 ml each of distilled water and saturated sodium chloride solution, dried over sodium sulfate and evaporated in vacuo. The residue was purified by flash chromatography on silica gel with a mixture of ethyl acetate/cyclohexane (2/1) containing 1% triethylamine as eluent, whereby 0.21 g (26% of theoretical) of the title compound was obtained as viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06656937B2 |
| Source dataset | uspto-grants-2003_12 |
| ORD ID | ord-1d089016284c484287a06a9baddc7555 |
| Source note | uspto-grants-2003_12 |